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FRESENIUS PUNCTUR-GUARD FISTULA NEEDLE SETS

K023162 Class II Traditional
Decision Date
2003-03-20
Sponsor / Applicant
Fresenius Medical Care

Technical Specification

510(k) Submission ID K023162
Product Code FIE
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5540
Decision Date 2003-03-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FRESENIUS PUNCTUR-GUARD FISTULA NEEDLE SETS received FDA 510(k) clearance under submission number K023162, sponsored by Fresenius Medical Care. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2003-03-20.

Classification & Regulation

This clearance is catalogued under FDA product code FIE and 21 CFR 876.5540, within the Gastroenterology, Urology review panel as a Class II device.